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SARS-CoV-2 infection in patients with β-thalassemia: The French experience
Estelle Jean-Mignard1, Gonzalo De Luna2, Laurent Pascal3
1Département de médecine interne, hôpital de la Timone, Assistance Publique des hôpitaux de Marseille, Marseille, France; Centre de référence des syndromes drépanocytaires majeurs, thalassémies et autres pathologies rares du globule rouge et de l'erythropoïèse, Assistance Publique des hôpitaux de Marseille, 264, rue Saint-Pierre, 13005 Marseille, France.
Insights
Patients with beta-thalassemia experienced mild to moderate COVID-19, with no deaths or severe complications reported. This study highlights the importance of monitoring for adverse events in these patients during viral infections.
Area of Science:
- Hematology
- Infectious Diseases
- Public Health
Background:
- Patients with severe thalassemia face increased risks due to iron overload, thrombosis, and infection.
- COVID-19 may pose a heightened risk to individuals with thalassemia.
Purpose of the Study:
- To investigate the clinical outcomes of COVID-19 in patients with beta-thalassemia.
Main Methods:
- A national survey in French reference centers identified 16 beta-thalassemia patients with confirmed COVID-19.
- Data collected included patient demographics, transfusion status, splenectomy, iron overload complications, and COVID-19 severity.
Main Results:
- 16 beta-thalassemia patients (11 months-60 years) had COVID-19; 15 were transfusion-dependent, 6 splenectomized.
- Most patients had mild symptoms; 3 developed pneumonia requiring oxygen but not ventilation.
- No thrombosis, organ failure, or death occurred; all patients recovered. Neutropenia was noted in 2 patients on specific treatments.
Conclusions:
- COVID-19 severity in this thalassemia cohort was mild to moderate, potentially higher than the general population but consistent with prior reports.
- Viral infections may increase the risk of adverse events from chronic thalassemia treatments.
Introduction:
Because of iron overload complications, thrombosis and infectious predisposition, patients with severe forms of thalassemia are likely to be at increased risk of COVID-19 complications.
Results:
A national survey conducted during the year 2020 across the French reference centers for hemoglobinopathies identified 16 cases of COVID-19 confirmed by RT-PCR in beta-thalassemia patients. Their age ranged from 11 months to 60 years. 15 patients were transfusion-dependent and 6 were splenectomized. Concerning iron overload related complications, none had diabetes or cirrhosis and only one had experienced heart failure. All 4 pediatric patients were pauci-symptomatic during the viral episode. Three patients (41, 49 and 57 years old) developed COVID-19 pneumonia requiring oxygen therapy without the need for mechanical ventilation. Neutropenia (absolute neutrophils count <0.5 10 9/L) was observed in 2 patients receiving long-term treatment with hydroxycarbamide and deferiprone. No thrombosis event, organ failure or death occurred. All patients recovered.
Conclusion:
Severity of COVID-19 in this population of young and middle-aged patients appeared increased compared to the general population but remained mild to moderate as already described in the few series reported in the literature. Occurrence of adverse events related to chronic treatment administered in thalassemia disease may be favored by the infectious episode.
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